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(2R,4R)-2-Methylpiperidin-4-ol, a cyclic amine and alcohol with the chemical formula C6H13NO, features a piperidine ring structure. (2R,4R)-2-Methylpiperidin-4-ol is recognized for its potential in the pharmaceutical industry, medicinal chemistry, and drug development, serving as a valuable intermediate and building block in organic synthesis and chemical research.

89451-59-2

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89451-59-2 Usage

Uses

Used in Pharmaceutical Industry:
(2R,4R)-2-Methylpiperidin-4-ol is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows for the development of new therapeutic agents, contributing to the advancement of medicinal chemistry.
Used in Medicinal Chemistry:
(2R,4R)-2-Methylpiperidin-4-ol is utilized as a building block in the production of other chemical compounds, facilitating the creation of novel molecules with potential therapeutic properties.
Used in Drug Development:
(2R,4R)-2-Methylpiperidin-4-ol is employed in the field of drug development, where its unique structure aids in the design and synthesis of innovative pharmaceuticals, enhancing the discovery of new treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 89451-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,5 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89451-59:
(7*8)+(6*9)+(5*4)+(4*5)+(3*1)+(2*5)+(1*9)=172
172 % 10 = 2
So 89451-59-2 is a valid CAS Registry Number.

89451-59-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Piperidinol, 2-methyl-, (2R-cis)-

1.2 Other means of identification

Product number -
Other names PBN20120722

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89451-59-2 SDS

89451-59-2Downstream Products

89451-59-2Relevant academic research and scientific papers

Aldolase-Catalyzed Asymmetric Synthesis of N-Heterocycles by Addition of Simple Aliphatic Nucleophiles to Aminoaldehydes

Roldán, Raquel,Hernández, Karel,Joglar, Jesús,Bujons, Jordi,Parella, Teodor,Fessner, Wolf-Dieter,Clapés, Pere

, p. 2673 - 2687 (2019/02/24)

Nitrogen heterocycles are structural motifs found in many bioactive natural products and of utmost importance in pharmaceutical drug development. In this work, a stereoselective synthesis of functionalized N-heterocycles was accomplished in two steps, com

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